Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.
about
A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype.Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations.
P2860
Three prevalent mutations in a patient with phenylalanine hydroxylase deficiency: implications for diagnosis and genetic counselling.
description
1996 nî lūn-bûn
@nan
1996 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Three prevalent mutations in a ...... nosis and genetic counselling.
@ast
Three prevalent mutations in a ...... nosis and genetic counselling.
@en
type
label
Three prevalent mutations in a ...... nosis and genetic counselling.
@ast
Three prevalent mutations in a ...... nosis and genetic counselling.
@en
prefLabel
Three prevalent mutations in a ...... nosis and genetic counselling.
@ast
Three prevalent mutations in a ...... nosis and genetic counselling.
@en
P2093
P2860
P356
P1476
Three prevalent mutations in a ...... nosis and genetic counselling.
@en
P2093
P2860
P304
P356
10.1136/JMG.33.2.161
P407
P577
1996-02-01T00:00:00Z